http://rdf.ncbi.nlm.nih.gov/pubchem/patent/JP-S6025954-A
Outgoing Links
Predicate | Object |
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assignee | http://rdf.ncbi.nlm.nih.gov/pubchem/patentassignee/MD5_88fbcd2a70a3c49d0aed69a000d55909 |
classificationIPCInventive | http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-313 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C67-31 http://rdf.ncbi.nlm.nih.gov/pubchem/patentipc/C07C69-675 |
filingDate | 1983-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
inventor | http://rdf.ncbi.nlm.nih.gov/pubchem/patentinventor/MD5_0c94b2e6304b3cb3233d4e66b4845c9b |
publicationDate | 1985-02-08-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
publicationNumber | JP-S6025954-A |
titleOfInvention | Production of acyloxyacetic acid compound |
abstract | PURPOSE: To produce an acyloxyacetic acid compound useful as a synthetic intermediate of various agricultural chemicals and pharmaceuticals, especially an intermediate of herbicides, in high efficiency, without using a catalyst, by reacting an α-halogenoacetic acid compound with a carboxylic acid salt in a specific solvent. n CONSTITUTION: The objective compound of formula III is produced by reacting the α-halogenoacetic acid compound of formula I [X is Cl or Br; R 1 and R 2 are H or alkyl; R 3 is OR' or NR"R'''(R' is alkyl; R" and R''' are H, alkyl or aryl)] with a carboxylic acid salt of formula II (R is H or alkyl; M is alkali metal or alkaline earth metal) in a solvent selected from dimethylsulfoxide, N,N-dimethylformamide, N,N-dimethylacetamide, hexamethylphosphoramide, acetonitrile and 1W3C lower alcohol, at 20W120°C. The amount of carboxylic acid salt can be reduced, and the formation of by-product caused by the polymerization of α- halogenoacetic acid can be suppressed. n COPYRIGHT: (C)1985,JPO&Japio |
priorityDate | 1983-07-20-04:00^^<http://www.w3.org/2001/XMLSchema#date> |
type | http://data.epo.org/linked-data/def/patent/Publication |
Incoming Links
Total number of triples: 25.